Home NDC 61010-1122-6 Saniwash Antimicrobial
Product NDC 61010-1122
Requested package NDC 61010-1122-6
11-digit product format 610101122
Labeler code 61010
Product ID 61010-1122_10a74b7b-a6c3-f224-e063-6294a90a4f67
Type HUMAN OTC DRUG
Nonproprietary name Chloroxylenol
Dosage form LIQUID
Route TOPICAL
Labeler Safetec of America, Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-04-22
Substance CHLOROXYLENOL
Active strength .006 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Saniwash Antimicrobial
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CHLOROXYLENOL .006 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 0F32U78V2Q Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# NDC, Effective, Related label table NDC Effective Related label 61010-1122-3 2024-02-13 61010-1122, Saniwash 61010-1122-4 2024-02-13 61010-1122, Saniwash 61010-1122-6 2024-02-13 61010-1122, Saniwash 61010-1122-7 2024-02-13 61010-1122, Saniwash 61010-1122-3 2024-01-30 61010-1122, Saniwash 61010-1122-4 2024-01-30 61010-1122, Saniwash 61010-1122-6 2024-01-30 61010-1122, Saniwash 61010-1122-7 2024-01-30 61010-1122, Saniwash
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 61010-1122-3 Saniwash Antimicrobial 473 mL in 1 BOTTLE, PUMP LIQUID 473 4 61010-1122-4 Saniwash Antimicrobial 800 mL in 1 BAG LIQUID 800 4 61010-1122-6 Saniwash Antimicrobial 3785 mL in 1 BOTTLE, PUMP LIQUID 3785 4 61010-1122-7 Saniwash Antimicrobial 208198 mL in 1 DRUM LIQUID 208198 4
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Chloroxylenol ACTIVE INGREDIENT 0F32U78V2Q SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 2 Chloroxylenol ACTIVE MOIETY 0F32U78V2Q SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 2 .ALPHA.-TOCOPHEROL ACETATE INACTIVE INGREDIENT 9E8X80D2L0 SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 2 Aloe Vera Leaf INACTIVE INGREDIENT ZY81Z83H0X SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 2 Cocamidopropyl Betaine INACTIVE INGREDIENT 5OCF3O11KX SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 2 COCO DIETHANOLAMIDE INACTIVE INGREDIENT 92005F972D SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 2 Diazolidinyl Urea INACTIVE INGREDIENT H5RIZ3MPW4 SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 2 EDETATE SODIUM INACTIVE INGREDIENT MP1J8420LU SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 2 Methylparaben INACTIVE INGREDIENT A2I8C7HI9T SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 2 Propylene Glycol INACTIVE INGREDIENT 6DC9Q167V3 SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 2 Propylparaben INACTIVE INGREDIENT Z8IX2SC1OH SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 2 Sodium Chloride INACTIVE INGREDIENT 451W47IQ8X SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 2 SODIUM LAURETH-3 SULFATE INACTIVE INGREDIENT BPV390UAP0 SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 2 Water INACTIVE INGREDIENT 059QF0KO0R SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61010-1122 SANIWASH ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 4 Current NDC, Legacy NDC, 4 package rows 20240214_6ac9df02-225d-4115-a9c6-a492faafe68a.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 61010-1122-6 61010112206 3785 mL in 1 BOTTLE, PUMP (61010-1122-6) 3785 ml 2014-04-22 0000-00-00 No No Current